Nickel-catalyzed exo-selective hydroacylation/Suzuki cross-coupling reaction.

Shao-Chi Lee, Lin Guo, Magnus Rueping

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


The first nickel-catalyzed intramolecular hydroacylation/Suzuki cross coupling cascade of o-allylbenzaldehydes with a broad range of phenylboronic acid neopentyl glycol esters has been developed. This strategy shows high regioselectivity and step economy in the construction of two C-C bonds via aldehyde C-H bond activation, affording valuable indanones with high efficiency.
Original languageEnglish (US)
Pages (from-to)14984-14987
Number of pages4
JournalChemical communications (Cambridge, England)
Issue number99
StatePublished - 2019

Bibliographical note

KAUST Repository Item: Exported on 2020-10-01


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